Max Factor Ltd
⚠️ Moderate Risk
FEI: 3004147022 • Naka, Ibaraki • JAPAN
FEI Number
3004147022
Location
Naka, Ibaraki
Country
JAPANAddress
1 Chome 17, Takenochi, Naka, Ibaraki, Japan
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/18/2004 | 66VBL99MISCELLANEOUS PATENT MEDICINES, ETC. | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 9/18/2004 | 53LY01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 9/18/2004 | 65LBL99PROTECTANT N.E.C. | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 9/18/2004 | 65LBL99PROTECTANT N.E.C. | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 9/18/2004 | 53LC01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Max Factor Ltd's FDA import refusal history?
Max Factor Ltd (FEI: 3004147022) has 5 FDA import refusal record(s) in our database, spanning from 9/18/2004 to 9/18/2004.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Max Factor Ltd's FEI number is 3004147022.
What types of violations has Max Factor Ltd received?
Max Factor Ltd has been cited for 1 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Max Factor Ltd come from?
All FDA import refusal data for Max Factor Ltd is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.